Xochiquetzallia | |
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Flower and umbel of Xochiquetzallia hannibalii with scale | |
Scientific classification | |
Kingdom: | Plantae |
Clade: | Tracheophytes |
Clade: | Angiosperms |
Clade: | Monocots |
Order: | Asparagales |
Family: | Asparagaceae |
Subfamily: | Brodiaeoideae |
Genus: | Xochiquetzallia J.Gut. |
Type species | |
Xochiquetzallia mortoniana (H.E. Moore) J.Gut. |
Xochiquetzallia is a genus of geophytic flowering plants of the subfamily Brodiaeoideae in the family Asparagaceae. [1] [2] The genus contains four species: three previously classified within the genus Dandya and one other previously classified within Milla . Earlier genetic and morphological research had shown that the broad Milla clade of plants is made up of two sister lineages. [3] The four plant species now within Xochiquetzallia make up one of these lineages, and are more closely related to each other than they are to the second lineage, which is made up of the remaining Milla species, Dandya purpusii , and the genera Behria , Bessera , Jaimehintonia and Petronymphe . [3] Jorge Gutiérrez and Teresa Terrazas, two of the botanists who worked on the earlier research, followed up in 2020 with a paper formally transferring the four species from Dandya and Milla to Xochiquetzallia. [1]
All four Xochiquetzallia species occur in Mexico's Río Balsas watershed, south of Mexico City.
Xochiquetzallia species are herbaceous perennials, growing from corms. They can be distinguished from related genera by the combination of two floral characteristics. The gynophore of a Xochiquetzallia flower lacks pith and the stigma is entire (undivided). Other genera in the Milla clade have pith in the gynophore and a divided stigma. [4]
Plants in this genus are between 20 cm and 60 cm high from the base of the corm to the top of the flowerhead. Their roots are fibrous and sometimes fleshy, emerging from a corm in the shape of a flattened ball that is between 1.0 cm and 2.5 cm in diameter. There are 5–9 narrow, dark-green leaves, each 20–49 cm long from the blunt base to the acute tip. In cross-section they may be flattened or somewhat circular (terete). The surface may be smooth (glabrous) or scaly (scabrous), with translucent projections along the leaf veins. The lower portions of the leaves arising from the corm form a brown tunic that surrounds the base of the scape (flower stalk) for up to 2.0 cm. [5]
The inflorescence is in the form of an umbel on top of a scape that is generally 20–50 cm long. This scape is cylindrical, usually shorter than the leaves, with a surface that is smooth with occasional acute prominences. Below the umbel there are 2–3 narrowly triangular bracts 3.0–9.0 mm long. There is also a single bracteole below each of the 4–20 flowers. The flowers are borne on pedicels 0.8–3.5 cm long arising from the top of the scape. In form they are either subcampanulate (broadly bell-shaped) or hypocrateriform (shaped like a salver on top of a narrow tube) and they are either held erect or droop somewhat from the tip of the pedicel. [5]
Flowers of Xochiquetzallia species are white or blue. Each begins with a tube (where the tepals are fused) that is 1–25 mm long. Like all lilioid monocots, the flowers have six tepals, arranged in two groups of three. Each outer tepal is elliptic in shape with a narrowing base, acute tip and 1–3 veins; these outer tepals measure 8.0–16.0 mm long and 2.0–7.0 mm wide. The inner three tepals are similar, but sometimes more broadly elliptical and with more obtuse tips; these inner tepals measure 8.0–16.0 mm long and 3.0–11.0 mm wide. The flower has six separate fertile stamens, each arising from a corresponding tepal near the throat of the floral tube. The stamen filaments are typically 2.0–5.0 mm long and may be thread-like or widen somewhat toward the base. Each of the six yellow anthers is 1.0–2.5 mm long and is basifixed (attached by its base to the stamen filament). The anthers taper towards the tip and sometimes towards the base as well. [6]
Among the female parts of the flower, the gynophore is 0.8–1.6 mm long. The ovary is cylindrical, 1.0–5.0 mm long, and fused at its base to the flower's perigone. Above this is a threadlike style 1.8–7.0 mm long bearing an undivided stigma with a bumpy surface. The fruit forms as a roughly ball-shaped or cylindrical, smooth-surfaced, brown, three-sided capsule 6.0–13.0 mm long. The capsule is loculicidal, meaning that when ripe it splits apart along the middle of each compartment. Inside are shiny black oblong or sickle-shaped seeds with a bumpy surface that are about 4.0 × 1.5 mm in size. [7]
Gutiérrez and Terrazas named the new genus for the Aztec goddess of flowers, Xōchiquetzal. [7] Xṓchitl means 'flower' in Nahuatl and quétzalli refers literally to the tail feathers of the quetzal bird, but also means 'precious'. Gutiérrez and Terrazas translate the combined word as 'beautiful flower'. [7]
Xochiquetzallia is one of 14 genera in the Brodiaeoideae subfamily within the Asparagaceae family of monocots. Within Brodiaeoideae, Xochiquetzallia is one of six genera in the Milla clade, which is centered in Mexico.
The Milla clade is estimated to have arisen approximately 15.8 Ma (15.8 million years ago) in the California Floristic Province, separating from the lineage that gave rise to the other eight genera within Brodiaeoideae. [8] From California, the Milla clade dispersed south and east to the Chihuahuan–Coahuila Plateaus and the Trans-Mexican Volcanic Belt and subsequently to Baja California and the Sierra Madre del Sur. [8]
Gutiérrez and Terrazas selected Xochiquetzallia mortoniana as the type species for the new genus. [7]
Gutiérrez and Terrazas transferred the following four species to the new genus:
The four species in Xochiquetzallia are all native to the broad Río Balsas valley in south-central Mexico. There are relatively few occurrence records for all four species.
Specimen records indicate that X. mortoniana and X. hannibalii grow in the lower reaches of the Río Balsas valley, in the states of Michoacán and Guerrero.
X. mortoniana was originally collected on the edge of cliffs at 1400 m elevation at Tierras Blancas, in Mina district of Guerrero. [9] Additional populations have been reported from lower down the valley in Michoacán.
X. hannibalii was originally recorded growing singly (rather than in clumps) in full sun and very light shade in gritty red soil on dry rocky hillsides facing west, in short grass near giant cacti. [10]
X. thadhowardii appears to be found further up the Río Balsas, at the Guerrero/Michoacán border and further east. The species was originally recorded in large colonies in part shade and full sun on hillsides with calcareous soil, growing under thorny shrubs and giant Neobuxbaumia tetetzo cacti. [11]
X. balsensis has been recorded only from tropical deciduous forest and thorn scrub above the Amacuzac River (a tributary of the Río Balsas) in Tlaquiltenango, Morelos, at an elevation of around 1200 m.
The distribution of X. thadhowardii and X. balsensis was originally thought to overlap and the two species are morphologically similar. When X. balsensis was described in 1992 (under the name Dandya balsensis), it was distinguished from the species now named X. thadhowardii based on a smaller perigone, shorter filaments and style, and free anthers (whereas X. thadhowardii has connate anthers fused around the style). [12] [13] Later studies by Gutiérrez and collaborators suggested that there were no morphological or anatomical differences between the two species. [14] [15] [16] Subsequent analysis did show that one population of X. balsensis, from an upland area in the state of Morelos, can be distinguished from X. thadhowardii. [13] X. balsensis is now recognized to also have flowers with connate anthers, which separate during advanced anthesis. [13] Instead, the species is now distinguished by filaments no longer than 3 mm and style segments less than or equal to 4 mm long. [13]
All species of Xochiquetzallia are rare and none of them is commonly available in the horticultural trade. They are occasionally grown in botanical gardens.
Brodiaea, also known by the common name cluster-lilies, is a monocot genus of flowering plants.
Milla, the Mexican star, is a genus of monocotyledonous plants in the family Asparagaceae, subfamily Brodiaeoideae. They are native mostly to Mexico, with one species extending into Guatemala, Honduras, Arizona, Texas and New Mexico.
Triteleia is a genus of monocotyledon flowering plants also known as triplet lilies. The 16 species are native to western North America, from British Columbia south to California and east to Wyoming and Arizona, with one species in northwestern Mexico. However, they are most common in California. They are perennial plants growing from a fibrous corm roughly spherical in shape. They get their name from the fact that all parts of their flowers come in threes.
Brodiaeoideae are a monocot subfamily of flowering plants in the family Asparagaceae, order Asparagales. They have been treated as a separate family, Themidaceae. They are native to Central America and western North America, from British Columbia to Guatemala. The name of the subfamily is based on the type genus Brodiaea.
Dipterostemon is a monotypic genus of flowering plants in the family Asparagaceae. Its only species is Dipterostemon capitatus, synonym Dichelostemma capitatum, known by the common names blue dicks, wild hyacinth, purplehead and brodiaea, native to the Western United States and northwest Mexico.
Triteleia ixioides, known as prettyface or golden star, is a monocotyledon flowering plant in the genus Triteleia. It is native to northern and central California and southwestern Oregon, where it can be found in coastal and inland coniferous forests and other habitat. It is a perennial wildflower growing from a corm. It produces one to two basal leaves up to 50 centimeters long by 1.5 wide. The inflorescence arises on an erect stem up to 80 centimeters tall. It is an umbel-like cluster of several flowers each borne on a pedicel up to 7 centimeters long. The flowers are variable in size, measuring one to nearly three centimeters in length. They are pale to bright yellow, or sometimes purple-tinged white. There are six tepals with darker midveins in shades of green, brown, or purple. The lobes are funnel-shaped and may open flat or somewhat reflexed. The six stamens form a fused tube that protrudes from the corolla; they have broad, flat filaments and whitish, yellowish, or blue anthers.
Brodiaea orcuttii is a species of flowering plant in the family Asparagaceae, within the subfamily Brodiaeoideae. It is a cluster-lily known by the common name Orcutt's brodiaea. This corm-sprouting species is nearly endemic to San Diego County, with the periphery of its range reaching the southern portion of Riverside County along with some populations sparsely scattered in northwestern Baja California. Brodiaea orcuttii is usually associated with the marginal areas of vernal pools, seeps, meadows, and stream embankments, microhabitats which can generally be found from coastal mesas to interior mountains. The red-purple to blue flowers bloom from April to July. It can be distinguished from all other species of Brodiaea by its lack of staminodes.
Dandya purpusii is a species of flowering plant endemic to northeast Mexico. It is the only species in the genus Dandya. In the APG III classification system, it is placed in the asparagus family Asparagaceae, and the cluster lily subfamily Brodiaeoideae. The genus is named in honor of James Edgar Dandy.
Petronymphe is a genus of flowering plants endemic to Mexico. It is placed in the family Asparagaceae, subfamily Brodiaeoideae.
Babiana ambigua is a species of plant in the Iridaceae. It is endemic to the Western Cape province of South Africa. It is a geophyte, that appears from an underground corm every year and grows to a height of 5–8 cm (2.0–3.1 in) or occasionally up to 16 cm (6.3 in). Its leaves are pleated, hairy, lance-shaped, reaching higher than the inflorescence. The fragrant, mirror-symmetric, blue to mauve flowers, consist of six tepals merged into a tube at their base, but with free lobes at the top. The lower lateral tepals have whitish markings accentuated by a more intense blue line along their margin. Each flower is supported by two green bracts sometimes with a brownish tip, and the inner bract is divided entirely to its base. There are three anthers crowded to the dorsal side of the perianth and a style divided in three branches on top of a smooth ovary. Flowers can be found from late July at sea level to the end of September at high altitude.
Dilatris is a genus of four species of evergreen perennial herbaceous plants of up to 60 cm (2.0 ft) high, that are assigned to the bloodroot family. The plants have hairless, line- to lance-shaped leaves set in a fan that emerges from a red or orange coloured rootstock. Six free tepals with some gland dots near their tips are present on the mauve or dirty yellow flowers' six free petals. The other two stamens are longer and spreading with smaller scarlet anthers, while the one stamen is short, upright, and has a large, yellow anther. The style is diverted from the centre opposite both longer stamens. The species only occur in the Western Cape and Northern Cape provinces of South Africa.
The Asparagales are an order of plants, and on this page the structure of the order is used according to the APG III system. The order takes its name from the family Asparagaceae and is placed in the monocots. The order is clearly circumscribed on the basis of DNA sequence analysis, but is difficult to define morphologically, since its members are structurally diverse. The APG III system is used in World Checklist of Selected Plant Families from the Royal Botanical Gardens at Kew. With this circumscription, the order consists of 14 families with approximately 1120 genera and 26000 species.
Allioideae is a subfamily of monocot flowering plants in the family Amaryllidaceae, order Asparagales. It was formerly treated as a separate family, Alliaceae. The subfamily name is derived from the generic name of the type genus, Allium. It is composed of about 18 genera.
Crocus ochroleucus is species of flowering plant in the Iridaceae family. It is a cream-colored crocus native to Lebanon, Palestine and Syria.
Muilla lordsburgana is a species of flowering plant known by the common name Lordsburg noino. It is native to the eastern fringe of the Chihuahuan Desert of southwestern New Mexico, where it is found in scrub habitats atop Lordsburg Mesa. It is a perennial growing from a corm and reaching no more than 9 centimeters in height. The flowering stem bears an umbel-shaped array of up to 6, but usually fewer, flowers on pedicels up to 2 centimeters long. Each flower has six tepals which are white to pale lavender in color with a prominent green midvein. At the center of the flower are six stamens with wide white to pale lavender petal-like filaments. The filaments are partially fused into an erect, cylindrical "crown".
Babiana rubrocyanea is a perennial geophyte of 5–15 cm (2.0–5.9 in) high, with entire, lance-shaped, hairy, pleated leaves and flowers that have a narrowly funnel-shaped tube at their base and six free tepal lobes at the top that form a wide cup that is purplish blue with a sharply defined carmine red centre. It can be found in a small area of the Western Cape province of South Africa. Flowers can be found from August to the middle of September. It is called blue-and-red babiana in English and rooibloubobbejaantjie in Afrikaans.
Babiana pygmaea is a perennial plant of about 10 cm (3.9 in) high that annually forms leaves and flowers from an underground corm that is assigned to the iris family. It has bowl-shaped, pale yellow flowers with six perianth lobes, purplish in its heart, emerging from a cylindrical tube, and lance-shaped, pleated and heary leafblades that are almost at a right angle with the sheaths. The species can be found in the Western Cape province of South Africa. It is called geelbobbejaantjie in Afrikaans.
Babiana cinnamomea is a perennial plant of about 4–6 cm (1.6–2.4 in) high that annually forms leaves and flowers from an underground corm that is assigned to the iris family. It has inconspicuous pale greenish yellow flowers and broad, hairless, pleated leaves with undulating margins. Flowers may be found in May and June. It occurs in the very north of the Western Cape province of South Africa.
Babiana hypogaea is a perennial plant of about 5–8 cm (2.0–3.1 in) high that annually forms leaves and flowers from an underground corm that is assigned to the iris family. It has pale greenish yellow, buff or rarely white, mirro-symmetrical flowers and line- to sickle-shaped, slightly pleated, thinly hairy or hairless leaves that are held horizontally or inclined, that grows in the summer rainfall areas of southeastern Namibia and central and northern central South Africa. Flowers may be found between June and September and sometimes between December and May. It is called Bobbejaankalkoentjie, Bobbejaanuintjie or Ertappeluintjie in Afrikaans.
Babiana mucronata is a perennial plant species that grows to about 5–18 cm (2.0–7.1 in) high and annually forms leaves and flowers from an underground corm. It is assigned to the iris family. It has a simple or branched, more or less upright spike of 3-12 dark to pale violet-blue, mirror-symmetrical flowers. Each flower consists of a perianth that is merged below into a funnel-shaped tube of 10–25 mm (0.39–0.98 in) long but splits into six unequal tepals. Three stamens are curved, crowded near the upper lip, and carry pale violet anthers. Flowers may be found between late July and September.